CLINICAL RESEARCH REGULATORY COORDINATOR III

The University of Alabama at Birmingham (UAB), O'Neal Comprehensive Cancer Center is seeking a Clinical Research Regulatory Coordinator III.

The O'Neal Comprehensive Cancer Center is one of 51 NCI-designated comprehensive cancer centers in the United States and is the only one in Alabama and in the Deep South region. A comprehensive designation also means UAB Medicine patients have access to leading-edge treatments or clinical trials that they may not otherwise have at local community hospitals or smaller cancer centers. For many, an NCI designation can hold the key to survival. On campus and around Birmingham, the O'Neal Cancer Center is a significant part of our economic powerhouse. The O'Neal Cancer Center powers more than 400 scientists and physician-scientists, cares for 20,000 patients annually, and is home to more than 160 employees, plus all the physicians and clinical staff engaged in cancer patient care. The link to our website is: https://www.uab.edu/onealcancercenter/

Please attach a current resume with this application.

General Responsibilities

• To prepare and submit multiple levels of research documentation (i.e. IRB submissions, educational materials, reports, grant renewal reports, and study forms).
• To prepares and maintain FDA applications for Investigational New Drugs (INDs) and Investigational Device Exemptions (IDEs).
• To lead the implementation of study specific regulatory processes of a moderate to complex nature.
• To conduct internal quality assurance audits of regulatory files as well as programs, reports, and teams working within clinical trial operations.
• To design and implement quality initiatives ensuring effective and efficient clinical processes.

Key Duties & Responsibilities

1. Prepares and submits multiple levels of research documentation (i.e., IRB submissions, educational materials, reports, grant renewal reports, and study forms). Prepares and maintains FDA applications for INDs and IDEs. Leads the implementation of study-specific regulatory processes of a moderate to complex nature.
2. Conducts internal quality assurance audits of regulatory files as well as programs, reports, and teams working within clinical trial operations. Designs and implements quality initiatives, ensuring effective and efficient clinical processes.
3. Writes reports, business correspondence, and procedure manuals. Plans, develops, and presents training. Develops and oversees the implementation of Standard Operating Procedures (SOPs) when needed. Improves processes as needed.
4. Serves as a mentor to junior regulatory staff. Trains others in various work responsibilities and provides constructive feedback. Serves as liaison with medical staff, University Departments, ancillary departments, satellite facilities, IRB, and sponsor contacts.
5. Plans, develops, and presents training. Ensures research staff complete all requisite training. Maintains appropriate licensure for clinicians.
6. Serves on various committees as appropriate. Stays active in relevant regional and national forums.
7. Performs other duties as assigned.

Annual Salary Range: $55,180 - $89,670

Qualifications

Bachelor's degree in a related field and five (5) years of related experience required. Work experience may NOT substitute for education requirement. Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) certification preferred.

Preferences

• Knowledge of ICH-GCP guidelines.
• IRB regulatory experience, FDA knowledge.
• Critical thinking skills.
• Problem-solving skills across a wide variety of clinical studies.
• Expert knowledge of related scientific and clinical terminology.
• Leadership skills.
• Ability to work independently as well as within a team.
• Negotiation skills.
• Presentation skills.
• Prioritization skills.
• Organizational skills.
• Process improvement and quality skills.
• Written and verbal communication skills.
• Prefer a health, science, or business administration degree.